MECHANISMS OF THE NATRIURETIC EFFECTS OF NEUTRAL ENDOPEPTIDASE INHIBITION IN DAHL SALT-SENSITIVE AND SALT-RESISTANT RATS

被引:11
|
作者
HIRATA, Y [1 ]
SUZUKI, E [1 ]
HAYAKAWA, H [1 ]
MATSUOKA, H [1 ]
SUGIMOTO, T [1 ]
KANGAWA, K [1 ]
MATSUO, H [1 ]
机构
[1] NATL CARDIOVASC CTR,RES INST,OSAKA,OSAKA,JAPAN
关键词
ATRIAL NATRIURETIC PEPTIDE; BRAIN NATRIURETIC PEPTIDE; CLEARANCE RECEPTOR; CYCLIC GMP;
D O I
10.1097/00005344-199402000-00016
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To explore the mechanisms of the renal effects of neutral endopeptidase (NEP) inhibition, the effects of an NEP inhibitor, candoxatril (UK 79,300; UK), in Dahl salt-sensitive (SS) and salt-resistant (SR) rats were examined. UK dose-dependently decreased blood pressure (BP) in SS rats (20 mg/kg: 174 +/- 5 vs. 155 +/- 8 mm Hg, p < 0.01) but not in SR rats. Urinary sodium excretion (UNaV) of both rat strains receiving high-salt diets was increased to a greater extent than that of rats receiving low-salt diets. Basal plasma atrial natriuretic peptide (ANP) level in hypertensive SS rats was higher than in SR rats (192 +/- 18 vs. 118 +/- 24 pg/ml, p < 0.05). UK increased ANP levels in the plasma and urine two- and 11-fold, respectively. UK-induced increases in UNaV, urinary cyclic GMP, and plasma ANP concentrations were significantly augmented by coadministration of a clearance receptor agonist, C-ANF(4-23) or brain natriuretic peptide (BNP). Thus, the effects of NEP inhibition appear to be potentiated by the reduced receptor-mediated metabolism of ANP. This may explain the greater response to the NEP inhibitor in Dahl rats with hypertension or high-salt feeding.
引用
收藏
页码:283 / 290
页数:8
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